Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 151590737 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||||
|
6 | 151526832 | intron variant | C/A | snv | 0.46 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
6 | 151551313 | intron variant | G/T | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
6 | 151569654 | intron variant | C/T | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
6 | 151575100 | intron variant | G/A | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
0.882 | 0.160 | 6 | 151612040 | intron variant | A/G | snv | 0.58 |
|
0.800 | 1.000 | 3 | 2008 | 2009 | ||||||||
|
0.851 | 0.160 | 6 | 151615542 | missense variant | G/A | snv | 0.31 | 0.36 |
|
0.800 | 1.000 | 2 | 2009 | 2009 | |||||||
|
6 | 151611643 | intron variant | A/G | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
6 | 151618046 | missense variant | G/A | snv | 0.49 | 0.57 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
6 | 151618425 | 3 prime UTR variant | T/C | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
6 | 151618635 | 3 prime UTR variant | T/C | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
11 | 46827809 | intron variant | G/A | snv | 0.64 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
8 | 119032590 | intron variant | G/A;C | snv |
|
0.800 | 1.000 | 3 | 2008 | 2009 | |||||||||||
|
1.000 | 0.080 | 8 | 119039999 | intron variant | T/C | snv | 0.60 |
|
0.800 | 1.000 | 3 | 2008 | 2009 | ||||||||
|
8 | 118963431 | intergenic variant | C/T | snv | 0.34 |
|
0.700 | 1.000 | 2 | 2009 | 2009 | ||||||||||
|
8 | 118996132 | intron variant | T/C | snv | 0.62 |
|
0.700 | 1.000 | 2 | 2009 | 2009 | ||||||||||
|
8 | 119027942 | intron variant | C/T | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
8 | 119022148 | intron variant | A/G | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
8 | 119027482 | intron variant | T/C | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
8 | 118960457 | intergenic variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||||
|
8 | 119021759 | intron variant | C/T | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
8 | 119008679 | intron variant | C/G | snv | 0.62 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
8 | 119041104 | intron variant | C/A | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
8 | 118991488 | upstream gene variant | C/G | snv | 0.61 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
8 | 119000461 | intron variant | C/G | snv | 0.65 |
|
0.800 | 1.000 | 1 | 2009 | 2018 |